DIC + Sickle Cell Flashcards

1
Q

What is ITP?

A

Idiopathic thrombocytopenia purpura
Low platelets causing purpuric rash
Autoimmune
Treat with steroids, immunoglobulins + platelets

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2
Q

What is DIC?

A

Disseminated intravascular coagulation
Clots formed in small vessels, using up platelets + clotting factors so bleeding occurs elsewhere (bleeding in skin, haematuria etc)

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3
Q

What scoring system is used for DIC?

A

ISTH

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4
Q

When should a platelet transfusion be given in DIC?

A

Pts bleeding or high risk of bleeding + platelet count <50

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5
Q

When is fresh frozen plasma given to pts with DIC?

A

Bleeding pts with DIC + prolonged PT + aPTT

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6
Q

When should heparin be given in DIC?

A

If thrombosis predominates:
VTE, purpura fulminans, ischemia, vascular skin infarction

Use continuous infusion of unfractionated heparin due to short half life + reversibility

Can be given as prophylaxis in non-bleeding pts against VTE

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7
Q

What should pts with DIC + sepsis be treated with?

A

Recombinant human activated protein C

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8
Q

Causes of DIC

A
Sepsis (gram negative)
Trauma 
Obstetric complications 
Pancreatitis 
Malignancy 
Nephrotic syndrome 
Transfusion 

(STOP Making New Thrombi)

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9
Q

S+S sickle cell disease

A

Recurrent haemolysis

Thrombosis in mesenteric, intracranial + bone = severe pain

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10
Q

Pathology of sickle cell

A

HbS inherited instead of HbA
Caused by mutations on B-globin gene
Distorts RBC in sickle shape which form clusters
Sickled cells have decreased lifespan, resulting in blood vessel occlusion + ischaemia, infections + pain in liver + spleen
Exacerbated by low O2 tension, dehydration + cold

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11
Q

Why will a newborn with sickle cell disease initially be asymptomatic?

A

The newborn still has increased levels of hemoglobin F and will be asymptomatic until his hemoglobin F is replaced by hemoglobin S

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12
Q

What is sickle cell anemia vs trait?

A
Anemia = Hb SS
Trait = Hb AS
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13
Q

Presentation of sickle cell disease

A
9-18 months
Painful dactylitis (swelling of bones of digits) 
Sudden severe infections 
Features of an acute crisis
Chronic anemia
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14
Q

Management of sickle cell

A

Immunisations
Abx prophylaxis
Pain relief for crisis

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